Verteporfin - another fibrotic inhibitor of specific to Peyronies Disease. Study says it works.

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Dipstick

Check this out guys,

Looks relatively new. https://www.researchgate.net/publication/327961732_Verteporfin_as_a_Medical_Treatment_in_Peyronie's_Disease

Another fibrosis inhibitor. I'm pretty sure long term use with these types of creams will eventually reduce the fibrosis surely.  
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melting

Great find!
verteporfin molecular weight:
718.794 g/mol

Maybe possible for transdermal(for example + DMSO) delivery.
Daily Transdermals and Traction/VED solved my Peyronies Disease https://www.peyroniesforum.net/index.php/topic,12587.0.html (DMSO+X)

samsung

45 y.o. Single. Onset of symptoms (pain-stinging like a wasp) @ 6/2018. No sudden injury. Curve developed slowly. 40 deg. dorsal. Hourglassing. Torsion to left flaccid. 4 rounds xiaflex. Restorex, DMSO+, heat, arginine, cialis, lipoic acid, vit. K2

projectpd

Age 57, Onset 2010, 2" shortening, shrinking and angulation of glans, weaker erections, 30 degree bend. Mild pain few months, but far from worst symptom. Tried many ideas, not just from here, but not consistently. Moderate improvement, maybe 40%

Bud luck

If it works, why the "uros" do not prescribe them? The same with heat therapy, nobody talks about it, but in one study showed great benefits. I feel like nobody cares about finding solutions, just us, this is devastating
My first symptoms started early in 2019
I tried Traction device, Pentofixiline, Q10, TRT, L-Argenine, cialis
I have narrowing/dent/hinge on the left side of my shaft
My ED is getting worse
Had a PRP shot Aug 2021
I have a girlfriend
Age 46

pey ron

I tried bringing this study up with an uro ~2 years ago. He didn't want to hear about it. If you can find a doctor with an open mind please let us know.
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